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<(6-Cyan-2-indolyl)methyl>triphenylphosphoniumbromid, with the molecular formula C33H25BrN2P, is a phosphonium salt that features a triphenylphosphonium cation and a 6-cyan-2-indolyl)methyl anion. This chemical compound is widely recognized for its role in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its versatile reactivity and functional groups make it a valuable component in the development of pharmaceuticals, agrochemicals, and materials science.

104291-64-7

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104291-64-7 Usage

Uses

Used in Organic Synthesis:
<(6-Cyan-2-indolyl)methyl>triphenylphosphoniumbromid is used as a reagent for constructing carbon-carbon and carbon-heteroatom bonds in organic synthesis. Its application is crucial in various reactions, including the Heck reaction and Suzuki-Miyaura coupling, which are metal-catalyzed cross-coupling reactions. <(6-Cyan-2-indolyl)methyl>triphenylphosphoniumbromid's ability to facilitate these reactions makes it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, <(6-Cyan-2-indolyl)methyl>triphenylphosphoniumbromid is utilized as a key intermediate in the synthesis of various drug candidates. Its unique reactivity and functional groups enable the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, this phosphonium salt is employed as a building block for the synthesis of new agrochemicals. Its application in this field contributes to the development of innovative products with enhanced performance and reduced environmental impact.
Used in Materials Science:
<(6-Cyan-2-indolyl)methyl>triphenylphosphoniumbromid also finds application in the field of materials science, where it is used to create new materials with specific properties. Its versatile reactivity allows for the development of materials with tailored characteristics, such as improved conductivity, stability, or mechanical strength.

Check Digit Verification of cas no

The CAS Registry Mumber 104291-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,9 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104291-64:
(8*1)+(7*0)+(6*4)+(5*2)+(4*9)+(3*1)+(2*6)+(1*4)=97
97 % 10 = 7
So 104291-64-7 is a valid CAS Registry Number.

104291-64-7Relevant academic research and scientific papers

Design, synthesis and biological activity of amidinobicyclic compounds (derivatives of DX-9065a) as factor Xa inhibitors: SAR study of S1 and aryl binding sites

Komoriya, Satoshi,Kanaya, Naoaki,Nagahara, Takayasu,Yokoyama, Asako,Inamura, Kazue,Yokoyama, Yukio,Katakura, Shin-Ichi,Hara, Tsuyoshi

, p. 2099 - 2114 (2007/10/03)

Since factor Xa (fXa) plays a pivotal role in the blood coagulation cascade, inhibition of fXa is thought to be an effective treatment for a variety of thrombotic events. (2S)-2-[4-[[(3S)-1-Acetimidoyl-3-pyrrolidinyl]oxy]phenyl] -3-(7-amidino-2-naphthyl)p

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